Vaccinium myrtillus

Vaccinium myrtillus - Leaf — Part: Leaf
Author: Sorin

Vaccinium myrtillus - Entire plant — Part: Entire plant
Author: Sorin

Upload a new image!

Details

Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

Contributors

Collections

Details Top

Internal ID	UUID643ffb0523e38864706770
Scientific name	Vaccinium myrtillus
Authority	L.
First published in	Sp. Pl. : 349 (1753)

Description Top

Suggest a correction or write a new one!

No description added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Vitis-idaea myrtillus	(L.) L.	Methodus : 47 (1794)
Myrtillus sylvaticus	Drejer	Fl. Excurs. Hafn. : 147 (1838)
Myrtillus niger	Gilib.	Fl. Lit. Inch. i. 4 (1781). 1782
Vaccinium oreophilum	Rydb.	Bull. Torrey Bot. Club 33: 148 (1906)
Vaccinium myrtillus var. oreophilum	(Rydb.) Dorn	Vasc. Pl. Wyoming 296 (1988):.
Myrtillus uliginosus var. microphylla	(Lange) Simmons	Nyt Mag. Naturvidensk. 41: 225 (1903)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	bilberry
English	whortleberry
English	european blueberry
English	hurt
English	blue whortleberry
English	common bilberry
English	fraughan
English	huckleberry
English	hurtleberry
English	urts
English	whinberry
English	whort
English	wimberry
English	winberry
English	blaeberry
Spanish	arándano
Spanish	arandano
Arabic	عنبية آسية
atj	minic
Azerbaijani	qaragilə
azb	قاراگیله
ba	Ҡара көртмәле
Belarusian	vaccínium myrtíllus
Belarusian	чарніцы
Bulgarian	черна боровинка
Tibetan	རྩི་ཤིང་རིགས་ཤིག
Bosnian	borovnica
bxr	Хара нэрhэн
Catalan	nabiu
Czech	brusnice borůvka
cv	Хура çырла
Welsh	llus
Danish	almindelig blåbær
German	heidelbeere
German	blaubeere, heidelbeere
German	blaubeere
Greek	Μύρτιλο
Esperanto	mirtelo
Estonian	harilik mustikas
Basque	ahabia
Persian	واکسینیوم میرتیلوس
Finnish	kangasmustikka
Finnish	mustikka
Faroese	bláber
French	myrtille commune
French	bleuet
French	myrtille
Irish	fraochán
Galician	arandeira
Hebrew	אוכמנית שחורה
Croatian	borovnica
Upper Sorbian	holanska jahodka
Hungarian	fekete áfonya
Armenian	հապալասի մրտենական
io	mirtelo
Icelandic	aðalbláber
Italian	mirtillo nero
Japanese	セイヨウスノキ
Korean	유럽블루베리
krc	Къара шкилди
kv	Чӧд
lb	molbier
lld	dlasenes
Lithuanian	mėlynė
Latvian	mellenes
myv	Пичечулякс
Norwegian Bokmål	blåbær
Norwegian Bokmål	skogsblåbær
Norwegian Bokmål	blåbærlyng
Dutch	blauwe bosbes
Norwegian Nynorsk	blåbær
olo	must'oi
os	Саунæмыг
pcd	grinbéle
Polish	czarna jagoda
Polish	borówka czarna
Pashto	اروپايي بلوبېري
Romanian	afin
Russian	ганабобель
Russian	гонобобель
Russian	черника миртолистная
Russian	черника обыкновенная
Russian	черника
rue	Яфина
rup	afinu
sco	blaeberry
se	sarri
Samogitian	mielīnė
Serbo-Croatian	borovnica
Slovak	čučoriedka obyčajná
Slovenian	borovnica
smn	sare
sms	sââʹrr
Albanian	boronica
Serbian	Боровница
stq	bikbäie
Swedish	blåbär
Turkish	yaban mersini
tt	Караҗиләк үсемлеге
udm	Кудымульы
Ukrainian	чорниця
vep	mustikaine
Vietnamese	việt quất quả đen
vro	mustik
Walloon	caclindjî
Chinese	米饭花果
Chinese	黑果越桔
Chinese	黑果越橘
Chinese	欧洲蓝莓

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Eastern Asia
  - Japan
- Middle Asia
  - Kazakhstan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Khabarovsk
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
- Western Asia
  - Turkey

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - North European Russia
  - Northwest European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Føroyar
  - Great Britain
  - Iceland
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Portugal
  - Spain

Northern America click to expand
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
- South-central U.S.A.
  - New Mexico
- Southwestern U.S.A.
  - Arizona
  - Nevada
  - Utah
- Subarctic America
  - Greenland
- Western Canada
  - Alberta
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000422209
UNII	EE76EZ4QNZ
Canadensys	5574
USDA Plants	VAMY2
Tropicos	12300055
INPN	128345
Flora of Italy	3740
KEW	urn:lsid:ipni.org:names:30006039-2
The Plant List	kew-2457648
Plantarium	39781
PFAF	Vaccinium myrtillus
Open Tree Of Life	817730
Observations.org	7602
NCBI Taxonomy	180763
NBN Atlas	NBNSYS0000003915
Nature Serve	2.135011
IPNI	30006039-2
iNaturalist	127029
GBIF	2882833
Freebase	/m/05pdbgg
FEIS	plants/shrub/vacmyr
EPPO	VACMY
EOL	583633
Elurikkus	8106
US Library of Congress	sh85141722
USDA GRIN	41040
Wikipedia	Vaccinium_myrtillus

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_016920895.1	VacMyr_v1.0	Chromosome	The New Zealand Institute for Plant and Food Research Limited	2021-02-23	100.0x	500.00 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Is the diet cyclic phase‐dependent in boreal vole populations?

Neby M, Ims RA, Kamenova S, Devineau O, Soininen EM

Ecol Evol

17-Apr-2024

PMCID:	PMC11024456
doi:	10.1002/ece3.11227

Verified hypotheses on the “nurse” and “burial” effects on introduced Quercus rubra regeneration in a mesic Scots pine forest

Woziwoda B, Dyderski MK, Gręda A, Frelich LE

Ecol Evol

01-Apr-2024

PMCID:	PMC10985384
doi:	10.1002/ece3.11185
PMID:	38571810

Bacterial and fungal communities in sub-Arctic tundra heaths are shaped by contrasting snow accumulation and nutrient availability

Männistö MK, Ahonen SH, Ganzert L, Tiirola M, Stark S, Häggblom MM

FEMS Microbiol Ecol

28-Mar-2024

PMCID:	PMC10996926
doi:	10.1093/femsec/fiae036
PMID:	38549428

Bioavailability and mechanisms of dietary polyphenols affected by non-thermal processing technology in fruits and vegetables

Liu Y, Deng J, Zhao T, Yang X, Zhang J, Yang H

Curr Res Food Sci

07-Mar-2024

PMCID:	PMC10951518
doi:	10.1016/j.crfs.2024.100715
PMID:	38511155

Exposure to Light of the Abaxial versus Adaxial Side of Detached Kalanchoë blossfeldiana Leaves Affects Anthocyanin Content and Composition Differently

Wiczkowski W, Saniewski M, Marasek-Ciołakowska A, Góraj-Koniarska J, Mitrus J, Horbowicz M

Int J Mol Sci

01-Mar-2024

PMCID:	PMC10932424
doi:	10.3390/ijms25052875
PMID:	38474120

Fecal DNA metabarcoding reveals seasonal and annual variation in willow ptarmigan diet

Ingvaldsen EW, Østnes JE, Kleven O, Davey M, Fossøy F, Nilsen EB

R Soc Open Sci

28-Feb-2024

PMCID:	PMC10898975
doi:	10.1098/rsos.231518
PMID:	38420626

The Antioxidant and Anti-Inflammatory Properties of Wild Bilberry Fruit Extracts Embedded in Mesoporous Silica-Type Supports: A Stability Study

Brezoiu AM, Deaconu M, Mitran RA, Sedky NK, Schiets F, Marote P, Voicu IS, Matei C, Ziko L, Berger D

Antioxidants (Basel)

19-Feb-2024

PMCID:	PMC10886266
doi:	10.3390/antiox13020250
PMID:	38397847

Specific Antimicrobial Activities Revealed by Comparative Evaluation of Selected Gemmotherapy Extracts

Héjja M, Mihok E, Alaya A, Jolji M, György É, Meszaros N, Turcus V, Oláh NK, Máthé E

Antibiotics (Basel)

13-Feb-2024

PMCID:	PMC10885950
doi:	10.3390/antibiotics13020181
PMID:	38391567

Influence of seasonality and biological activity on infection by helminths in Cantabrian bear

Valderrábano Cano E, Penteriani V, Vega I, Delgado MD, González-Bernardo E, Bombieri G, Zarzo-Arias A, Sánchez-Andrade Fernández R, Paz-Silva A

Int J Parasitol Parasites Wildl

09-Feb-2024

PMCID:	PMC10877405
doi:	10.1016/j.ijppaw.2024.100916
PMID:	38379728

Arthropod diversity in the alpine tundra using metabarcoding: Spatial and temporal differences in alpha‐ and beta‐diversity

Hein N, Astrin JJ, Beckers N, Giebner H, Langen K, Löffler J, Misof B, Fonseca VG

Ecol Evol

09-Feb-2024

PMCID:	PMC10857931
doi:	10.1002/ece3.10969
PMID:	38343576

Self-assembled, disordered structural color from fruit wax bloom

Middleton R, Tunstad SA, Knapp A, Winters S, McCallum S, Whitney H

Sci Adv

07-Feb-2024

PMCID:	PMC10849586
doi:	10.1126/sciadv.adk4219
PMID:	38324684

Effects of past and present habitat on the gut microbiota of a wild rodent

Scholier T, Lavrinienko A, Kallio ER, Watts PC, Mappes T

Proc Biol Sci

07-Feb-2024

PMCID:	PMC10846943
doi:	10.1098/rspb.2023.2531
PMID:	38320610

Investigation of volatile compounds during fermentation of Elaeagnus moorcroftii Wall.ex schlecht. juice by Bifidobacterium animalis subsp. lactis HN-3 and Lacticaseibacillus paracasei YL-29

Wang Y, Li W, Wang X, Hu Q, Kong J, wang X, Lan Z, Wang C, Zhang Y

Food Chem X

06-Feb-2024

PMCID:	PMC10869281
doi:	10.1016/j.fochx.2024.101171
PMID:	38370297

Element contents and their seasonal dynamics in leaves of alder Alnus glutinosa (L.) Gaertn

Hrdlička P, Kula E

Environ Monit Assess

01-Feb-2024

PMCID:	PMC10834585
doi:	10.1007/s10661-024-12367-x
PMID:	38300340

Vaccinium uliginosum L. (bog bilberry) and the search for its alleged toxicity: a review

Vaneková Z, Holloway P, Rollinger JM

Front Toxicol

31-Jan-2024

PMCID:	PMC10864615
doi:	10.3389/ftox.2024.1358840
PMID:	38357417

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3-Hydroxybenzoic acid	7420	Click to see C1=CC(=CC(=C1)O)C(=O)O	138.12	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane	12409	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC	408.80	unknown	https://doi.org/10.1002/JPS.3030430413
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
Secoisolariciresinol	65373	Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O	362.40	unknown	https://doi.org/10.1016/J.FOODCHEM.2012.03.133
Secoisolariciresinol-sesquilignan	59728532	Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)OC(CO)C(C3=CC(=C(C=C3)O)OC)O)OC)CO)O	558.60	unknown	https://doi.org/10.1016/J.FOODCHEM.2012.03.133
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1016/J.FOODCHEM.2012.03.133
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol	332427	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1016/J.FOODCHEM.2012.03.133
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(4R)-3-[(S)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one	101392635	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2C(C3=CC(=C(C=C3)O)OC)O)O	374.40	unknown	https://doi.org/10.1016/J.FOODCHEM.2012.03.133
Arctigenin methyl ether	384877	Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC)OC)OC	386.40	unknown	https://doi.org/10.1016/J.FOODCHEM.2012.03.133
Dimethylmatairesinol	1286	Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC)OC)OC	386.40	unknown	https://doi.org/10.1016/J.FOODCHEM.2012.03.133
Matairesinol	119205	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O	358.40	unknown	https://doi.org/10.1016/J.FOODCHEM.2012.03.133
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol	14521039	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O	552.60	unknown	https://doi.org/10.1016/J.PHYTOL.2011.02.002
Lyoniside	14521038	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O	552.60	unknown	https://doi.org/10.1016/J.PHYTOL.2011.02.002
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentan-2-yl 3-(4-hydroxyphenyl)prop-2-enoate	74178144	Click to see CC(CC(C)OC(=O)C=CC1=CC=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O	412.40	unknown	https://doi.org/10.1002/HLCA.200900220
4-Hydroxy-trans-cinnamic acid (1S,3R)-1-methyl-3-(beta-D-glucopyranosyloxy)butyl ester	38362480	Click to see CC(CC(C)OC(=O)C=CC1=CC=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O	412.40	unknown	https://doi.org/10.1002/HLCA.200900220
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
[(1S,5R,8R,9S,10R,11S,13R,14S,16S,17R,18S,19S)-10,13-dihydroxy-5-methyl-12-methylidene-3-oxo-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-19-yl] benzoate	101933335	Click to see CC12CC(=O)CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7O)OC(=O)C8=CC=CC=C8	447.50	unknown	https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1002/ARDP.19923250303 https://doi.org/10.1081/JLC-100101827 https://doi.org/10.1016/0003-2670(92)85082-H
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
2-(2-Hydroxyethyl)-3,4-bis(hydroxymethyl)cyclopent-3-en-1-ol	53462571	Click to see C1C(C(C(=C1CO)CO)CCO)O	188.22	unknown	https://doi.org/10.1016/S0731-7085(00)00264-8 https://doi.org/10.1076/PHBI.37.2.109.6091 https://doi.org/10.1002/ARDP.19923250303
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol	14985	Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C	430.70	unknown	https://doi.org/10.1002/HLCA.200900220
DL-alpha-Tocopherol	2116	Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C	430.70	unknown	https://doi.org/10.1002/HLCA.200900220
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,5R,6S,7R,7aS)-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-5,6,7-triol	162845885	Click to see CC1(C2C(C=COC2OC3C(C(C(C(O3)CO)O)O)O)C(C1O)O)O	364.34	unknown	https://doi.org/10.1248/CPB.52.226 https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1002/ARDP.19923250303 https://doi.org/10.1016/0003-2670(92)85082-H https://doi.org/10.1016/S0168-9452(97)00241-0 https://doi.org/10.1076/PHBI.37.2.109.6091
(1S,4aS,7R,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid	3488508	Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O	390.34	unknown	https://doi.org/10.1002/HLCA.200900220
Monotropein	73466	Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O	390.34	unknown	https://doi.org/10.1002/HLCA.200900220
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Lutein	5281243	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	https://doi.org/10.1016/S0168-9452(97)00241-0
Zeaxanthin	5280899	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C	568.90	unknown	https://doi.org/10.1016/S0168-9452(97)00241-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3R,4aR,6aR,6bR,8aR,11S,12S,12aS,14aS,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate	162999321	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C	468.80	unknown	https://doi.org/10.1081/JLC-100101827
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1002/HLCA.200900220
5-Glutinen-3-ol	12309493	Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1002/HLCA.200900220
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1002/HLCA.200900220
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1002/HLCA.200900220 https://doi.org/10.1002/JPS.3030430413
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1002/HLCA.200900220
Glutinol	9932254	Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C	426.70	unknown	https://doi.org/10.1002/HLCA.200900220
Olean-12-en-3beta-ol	225689	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1002/JPS.3030430413 https://doi.org/10.1002/HLCA.200900220
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1002/HLCA.200900220
Urs-12-en-3beta-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1002/HLCA.200900220
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1002/HLCA.200900220
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Macdougallin	23258271	Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3=C2CC(C4C3(CCC(C4)O)C)O)C)C	416.70	unknown	https://doi.org/10.1016/S0731-7085(00)00264-8 https://doi.org/10.1021/JF025781X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate	25180961	Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C	360.50	unknown	https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1016/S0168-9452(97)00241-0 https://doi.org/10.1076/PHBI.37.2.109.6091 https://doi.org/10.1016/0003-2670(92)85082-H https://doi.org/10.1002/ARDP.19923250303 https://doi.org/10.1248/CPB.52.226
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1002/HLCA.200900220 https://doi.org/10.1016/S0168-9452(97)00241-0
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0168-9452(97)00241-0
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1002/HLCA.200900220
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
Malic Acid	525	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1021/JF0205110
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
N-[1-[[1-[[1-[[1-[[1-[[1-[[1-[[3-[1-(dimethylamino)propan-2-ylamino]-3-oxopropyl]amino]-2-methyl-1-oxopropan-2-yl]amino]-2-methyl-1-oxopropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-2-methyl-1-oxopropan-2-yl]amino]-3-hydroxy-4-methyl-1-oxopentan-2-yl]amino]-6-hydroxy-4-methyl-1,8-dioxodecan-2-yl]-4-methyl-1-(4-methylhex-2-enoyl)pyrrolidine-2-carboxamide	156861	Click to see CCC(C)C=CC(=O)N1CC(CC1C(=O)NC(CC(C)CC(CC(=O)CC)O)C(=O)NC(C(C(C)C)O)C(=O)NC(C)(C)C(=O)NC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC(C)(C)C(=O)NC(C)(C)C(=O)NCCC(=O)NC(C)CN(C)C)C	1218.60	unknown	https://doi.org/10.1111/J.1750-3841.2010.01546.X
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
(2R)-1-[(2S,6S)-6-[(2S)-2-hydroxy-2-phenylethyl]-1-methylpiperidin-2-yl]propan-2-ol	163194695	Click to see CC(CC1CCCC(N1C)CC(C2=CC=CC=C2)O)O	277.40	unknown	https://doi.org/10.1248/CPB.52.226 https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1002/ARDP.19923250303 https://doi.org/10.1016/0003-2670(92)85082-H https://doi.org/10.1076/PHBI.37.2.109.6091
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1055/S-0028-1099474
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X https://doi.org/10.1055/S-0028-1099474
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2S,3S,4S,5R)-2,5-bis(hydroxymethyl)-2-methoxyoxolane-3,4-diol	6325664	Click to see COC1(C(C(C(O1)CO)O)O)CO	194.18	unknown	https://doi.org/10.1002/HLCA.200900220
methyl beta-D-fructofuranoside	128889	Click to see COC1(C(C(C(O1)CO)O)O)CO	194.18	unknown	https://doi.org/10.1002/HLCA.200900220
Methylbeta-D-fructofuranoside	14055124	Click to see COC1(C(C(C(O1)CO)O)O)CO	194.18	unknown	https://doi.org/10.1002/HLCA.200900220
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(4-Hydroxyphenoxy)-6-[3-(4-hydroxyphenyl)prop-2-enoxymethyl]oxane-3,4,5-triol	162890773	Click to see C1=CC(=CC=C1C=CCOCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O	404.40	unknown	https://doi.org/10.1021/JF025781X https://doi.org/10.1016/S0731-7085(00)00264-8 https://doi.org/10.1016/0003-2670(92)85082-H
2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol	346	Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O	272.25	unknown	https://doi.org/10.1007/BF00597526
Arbutin	440936	Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O	272.25	unknown	https://doi.org/10.1007/BF00597526
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
(2R)-2-[(5S,6R)-6-[(3E,5E)-6-[(1S,4S,5R)-1-ethyl-4-(1H-pyrrole-2-carbonyl)-2,3,3a,4,5,7a-hexahydro-1H-inden-5-yl]hexa-3,5-dien-3-yl]-5-methyloxan-2-yl]propanoic acid	163034766	Click to see CCC1CCC2C1C=CC(C2C(=O)C3=CC=CN3)C=CC=C(CC)C4C(CCC(O4)C(C)C(=O)O)C	493.70	unknown	https://doi.org/10.1016/0003-2670(92)85082-H https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1076/PHBI.37.2.109.6091 https://doi.org/10.1248/CPB.52.226 https://doi.org/10.1002/ARDP.19923250303
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2S,3S,4R,5R)-2-(hydroxymethyl)-2-methoxyoxane-3,4,5-triol	53655245	Click to see COC1(C(C(C(CO1)O)O)O)CO	194.18	unknown	https://doi.org/10.1002/HLCA.200900220
Methyl hex-2-ulopyranoside	219886	Click to see COC1(C(C(C(CO1)O)O)O)CO	194.18	unknown	https://doi.org/10.1002/HLCA.200900220
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,4S,5R,8S,10S,13S,14R,16R,17S,18R,19S,20R)-10,16-dihydroxy-4,5,13,19,20-pentamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one	163191286	Click to see CC1CCC23CCC4(C5(CCC6CC(CCC6(C5CC(C4(C2C1C)OC3=O)O)C)O)C)C	444.60	unknown	https://doi.org/10.1002/HLCA.200900220
10,16-Dihydroxy-4,5,13,19,20-pentamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one	162911875	Click to see CC1CCC23CCC4(C5(CCC6CC(CCC6(C5CC(C4(C2C1C)OC3=O)O)C)O)C)C	444.60	unknown	https://doi.org/10.1002/HLCA.200900220
3,6,6a-trimethyl-3a,4-dihydro-3H-cyclopenta[b]furan-2-one	163010358	Click to see CC1C2CC=C(C2(OC1=O)C)C	166.22	unknown	https://doi.org/10.1081/JLC-100101827
> Organoheterocyclic compounds / Quinolizines
(4S,9aR)-4-methyl-1,3,4,6,7,8,9,9a-octahydroquinolizin-2-one	13115690	Click to see CC1CC(=O)CC2N1CCCC2	167.25	unknown	https://doi.org/10.1016/0040-4020(81)85024-7
Myrtine	433955	Click to see CC1CC(=O)CC2N1CCCC2	167.25	unknown	https://doi.org/10.1016/0040-4020(81)85024-7
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Grossamide	101262727	Click to see COC1=CC(=CC2=C1OC(C2C(=O)NCCC3=CC=C(C=C3)O)C4=CC(=C(C=C4)O)OC)C=CC(=O)NCCC5=CC=C(C=C5)O	624.70	unknown	https://doi.org/10.1248/CPB.52.226 https://doi.org/10.1081/JLC-100101827 https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1002/ARDP.19923250303 https://doi.org/10.1016/0003-2670(92)85082-H https://doi.org/10.1076/PHBI.37.2.109.6091
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2S,4R)-4-hydroxypentan-2-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	102165886	Click to see CC(CC(C)OC(=O)C=CC1=CC=C(C=C1)O)O	250.29	unknown	https://doi.org/10.1002/HLCA.200900220
4-Hydroxypentan-2-yl 3-(4-hydroxyphenyl)prop-2-enoate	163036856	Click to see CC(CC(C)OC(=O)C=CC1=CC=C(C=C1)O)O	250.29	unknown	https://doi.org/10.1002/HLCA.200900220
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1055/S-0028-1099474
2-Hydroxycinnamic acid, (2E)-	637540	Click to see C1=CC=C(C(=C1)C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid	709	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1016/S0963-9969(00)00086-7
3'-Hydroxycinnamic acid	637541	Click to see C1=CC(=CC(=C1)O)C=CC(=O)O	164.16	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X https://doi.org/10.1055/S-0028-1099474
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1021/JF991274C https://doi.org/10.1021/JF025781X
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1021/JF991274C https://doi.org/10.1021/JF025781X
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1021/JF025781X https://doi.org/10.1016/S0963-9969(00)00086-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,3R,4S,5R,6R)-2-[2-(3,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	11340563	Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	479.40	unknown	https://doi.org/10.1248/CPB.52.628
(2S,3R,4S,5R,6R)-2-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	5484292	Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	493.40	unknown	https://doi.org/10.1081/JLC-100101827
(2S,3R,4S,5R,6S)-2-[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	154496514	Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	465.40	unknown	https://doi.org/10.1248/CPB.52.628
(2S,3R,4S,5R,6S)-2-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	154497274	Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	493.40	unknown	https://doi.org/10.1248/CPB.52.628
(2S,3S,4R,5R,6S)-2-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	154497174	Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O	463.40	unknown	https://doi.org/10.1248/CPB.52.628
(2S,5R)-2-[2-(3,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	44256953	Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	479.40	unknown	https://doi.org/10.1081/JLC-100101827
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	44256715	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1016/S0168-9452(97)00241-0 https://doi.org/10.1076/PHBI.37.2.109.6091 https://doi.org/10.1016/0003-2670(92)85082-H https://doi.org/10.1002/ARDP.19923250303 https://doi.org/10.1248/CPB.52.226
(2S,5S)-2-[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	44256883	Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	465.40	unknown	https://doi.org/10.1248/CPB.52.226
1-Benzopyrylium,3-(b-D-galactopyranosyloxy)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-	13915667	Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	465.40	unknown	https://doi.org/10.1016/0003-2670(92)85082-H https://doi.org/10.1076/PHBI.37.2.109.6091 https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1002/ARDP.19923250303
Cyanidin 3-O-galactoside	441699	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	https://doi.org/10.1248/CPB.52.628
Delphinidin 3-O-glucoside cation	443650	Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	465.40	unknown	https://doi.org/10.1076/PHBI.37.2.109.6091 https://doi.org/10.1248/CPB.52.628
Kuromanin	441667	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	https://doi.org/10.1248/CPB.52.628 https://doi.org/10.1021/JF900894K
Malvidin 3-O-beta-D-glucopyranoside	44256977	Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	493.40	unknown	https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1002/ARDP.19923250303 https://doi.org/10.1081/JLC-100101827 https://doi.org/10.1248/CPB.52.226 https://doi.org/10.1016/0003-2670(92)85082-H
Petunidin 3-galactoside	14311149	Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	479.40	unknown	https://doi.org/10.1248/CPB.52.226
Petunidin 3-glucoside	443651	Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	479.40	unknown	https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1002/ARDP.19923250303 https://doi.org/10.1081/JLC-100101827 https://doi.org/10.1248/CPB.52.226 https://doi.org/10.1016/0003-2670(92)85082-H https://doi.org/10.1076/PHBI.37.2.109.6091 https://doi.org/10.1248/CPB.52.628
Primulin	3568969	Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O	493.40	unknown	https://doi.org/10.1248/CPB.52.226 https://doi.org/10.1076/PHBI.37.2.109.6091
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R,4R,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxyoxane-3,4,5-triol	154497791	Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C=C4)O)O)O)O)O)O)O	419.40	unknown	https://doi.org/10.1248/CPB.52.628
(2R,3R,4R,5S)-2-[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxane-3,4,5-triol	163187218	Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O	435.40	unknown	https://doi.org/10.1248/CPB.52.628
(2R,3S,4R,5S)-2-[2-(3,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxyoxane-3,4,5-triol	154497194	Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(CO4)O)O)O)O)O	449.40	unknown	https://doi.org/10.1248/CPB.52.628
(2S,3R,4S,5R,6R)-2-[[2-(3,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-2H-chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	57357857	Click to see COC1=CC(=CC(=C1O)O)C2C(=CC3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1016/0003-2670(92)85082-H https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1076/PHBI.37.2.109.6091
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	5353915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/JA01097A013
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51402807	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/JA01097A013
2-[5,7-Dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxane-3,4,5-triol	22283733	Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O	435.40	unknown	https://doi.org/10.1081/JLC-100101827
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	12308704	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1021/JA01097A013
Avicularin	5490064	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1021/JA01097A013
delphinidin 3-O-beta-D-glucoside betaine	165559	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C=C3C(=CC(=O)C=C3O2)O)OC4C(C(C(C(O4)CO)O)O)O	464.40	unknown	https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1002/ARDP.19923250303 https://doi.org/10.1081/JLC-100101827 https://doi.org/10.1016/0003-2670(92)85082-H
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/JA01097A013
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1111/J.1365-2621.1987.TB14056.X https://doi.org/10.1021/JA01097A013
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
3,3',4',5,5',7-Hexahydroxyflavylium	128853	Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O	303.24	unknown	https://doi.org/10.1016/S0731-7085(00)00264-8 https://doi.org/10.1016/0003-2670(92)85082-H
Cyanidin	128861	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O)O	287.24	unknown	https://doi.org/10.1016/S0731-7085(00)00264-8 https://doi.org/10.1076/PHBI.37.2.109.6091 https://doi.org/10.1016/0003-2670(92)85082-H
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Malvidin	159287	Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O	331.30	unknown	https://doi.org/10.1016/S0731-7085(00)00264-8 https://doi.org/10.1021/JF025781X
Petunidin	441774	Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O	317.27	unknown	https://doi.org/10.1016/S0731-7085(00)00264-8 https://doi.org/10.1076/PHBI.37.2.109.6091 https://doi.org/10.1002/ARDP.19923250303
> Phenylpropanoids and polyketides / Macrolides and analogues
Avermectin A1b	9940924	Click to see CC1C=CC=C2COC3C2(C(C=C(C3OC)C)C(=O)OC4CC(CC=C(C1OC5CC(C(C(O5)C)OC6CC(C(C(O6)C)O)OC)OC)C)OC7(C4)C=CC(C(O7)C(C)C)C)O	873.10	unknown	https://doi.org/10.1016/S0021-9673(01)93636-2 https://doi.org/10.1016/S0168-9452(97)00241-0 https://doi.org/10.1002/ARDP.19923250303 https://doi.org/10.1076/PHBI.37.2.109.6091 https://doi.org/10.1016/0003-2670(92)85082-H
> Phenylpropanoids and polyketides / Stilbenes
Resveratrol	445154	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O	228.24	unknown	https://doi.org/10.1021/JF034150F
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	https://doi.org/10.1016/S0963-9969(00)00086-7

Biological Material Top

Contributors Top

Collections Top

In private collections	0
In public collections	1

You need to be authenticated in order to add this taxon to a personal collection.

Vaccinium myrtillus

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top